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在一名因甲状腺功能减退引发肾上腺危象而需要体外膜肺氧合(VA ECMO)的患者中启动左甲状腺素治疗:一个可预防的灾难故事。

Initiation of levothyroxine in a patient with hypothyroidism inducing adrenal crisis requiring VA ECMO: a tale of preventable disaster.

作者信息

Kang Mandip Singh, Sandhu Charnjeet Singh, Singh Natasha, Evans Timothy

机构信息

Internal Medicine, UCSF, Fresno, California, USA.

Pulmonary Medicine and Critical Care, UCSF, Fresno, California, USA.

出版信息

BMJ Case Rep. 2019 Aug 30;12(8):e230601. doi: 10.1136/bcr-2019-230601.

DOI:10.1136/bcr-2019-230601
PMID:31471362
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6721784/
Abstract

A 31-year-old man with a recent diagnosis of hypothyroidism presented to the emergency department as a transfer from the clinic for severe hypotension and hypoglycaemia. The patient endorsed a 2-week history of severe fatigue, weight loss, nausea and non-bloody emesis. He was aggressively hydrated and vasopressors were initiated. Despite these measures, the patient remained hypotensive and went into pulseless electrical activity. Return of spontaneous circulation was achieved via advanced cardiac life support protocol, and venous arterial extracorporeal membrane oxygenation (ECMO) was initiated. On day 3 of hospitalisation, the patient was weaned off ECMO support, and subsequent autoimmune work-up confirmed the diagnosis of autoimmune polyglandular syndrome type 2 with positive antiperoxidase antibodies (267 IU/mL), supporting the diagnosis of Hashimoto's thyroiditis.

摘要

一名31岁男性,近期诊断为甲状腺功能减退,因严重低血压和低血糖从诊所转诊至急诊科。患者自述有2周的严重疲劳、体重减轻、恶心和非血性呕吐病史。给予积极补液并开始使用血管升压药。尽管采取了这些措施,患者仍处于低血压状态,并出现了无脉电活动。通过高级心脏生命支持方案实现了自主循环恢复,并启动了静脉-动脉体外膜肺氧合(ECMO)。住院第3天,患者撤下ECMO支持,随后的自身免疫检查确诊为2型自身免疫性多腺体综合征,抗过氧化物酶抗体阳性(267 IU/mL),支持桥本甲状腺炎的诊断。

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本文引用的文献

1
A Case of Autoimmune Polyglandular Syndrome .ype 2 Associated with Atypical Form of Scleromyxedema.1例2型自身免疫性多腺体综合征合并非典型硬肿病样黏液水肿
Ethiop J Health Sci. 2016 Sep;26(5):503-507.
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Primary Adrenal Insufficiency Misdiagnosed as Hypothyroidism in a Patient with Polyglandular Syndrome.一名患有多腺体综合征的患者,原发性肾上腺功能不全被误诊为甲状腺功能减退症。
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A Case of Autoimmune Polyglandular Syndrome (APS) Type II with Hypothyroidism, Hypoadrenalism, and Celiac Disease - A Rare Combination.一例伴有甲状腺功能减退、肾上腺功能减退和乳糜泻的Ⅱ型自身免疫性多腺体综合征(APS)——一种罕见的组合。
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